Performance and Nutrition Program for Athletes in Adaptive Sports
NCT ID: NCT03392155
Last Updated: 2019-06-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
15 participants
INTERVENTIONAL
2018-01-09
2019-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
OTHER
NONE
Study Groups
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Training & Nutrition
Participants receive performance training twice a week for 12 weeks and group and individual nutritional counseling during the 12 weeks.
Training & Nutrition
Exercise at moderate to high intensities and diet education/counseling
Interventions
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Training & Nutrition
Exercise at moderate to high intensities and diet education/counseling
Eligibility Criteria
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Inclusion Criteria
* Participants with traumatic or non-traumatic spinal cord injury
* Able to perform progressive exercise program
* Willingness to participate in study
Group 2 (Able-bodied group):
* Functional upper extremity range of motion
* Able to perform progressive exercise program
* Willingness to participate in study
Group3 (Other physical disability group):
* Participants with a physical disability other than spinal cord injury
* Able to perform progressive exercise program
* Willingness to participate in study
Exclusion Criteria
• Any documented or reported health condition that would be contraindicated to a progressive exercise program
18 Years
70 Years
ALL
Yes
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Meegan G. Van Straaten
Principal Investigator
Principal Investigators
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Meegan G Van Straaten
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic in Rochester
Rochester, Minnesota, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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17-005392
Identifier Type: -
Identifier Source: org_study_id
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